Taiwan FDA registration 14d3ff7815d167af8643218f2493cd55

"Kawasumi" hemodialyzer

TW: "川澄"血液透析器
Taiwan flagTaiwan·Risk Class 2·KAWASUMI LABORATORIES,INC. MIE FACTORY·Registered Aug 18, 2006 – Aug 18, 2011Cancelled
Registration details
Analysis ID
14d3ff7815d167af8643218f2493cd55
Customs Code
DHA00601701807
Company information
Manufacturer Country
Japan
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.5860 高滲透性之血液透析系統
Import Information
import
Dates and status
Registration Date
Aug 18, 2006
Expiry Date
Aug 18, 2011
Cancellation Date
Jan 14, 2013
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Kawasumi" hemodialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14d3ff7815d167af8643218f2493cd55 and manufactured by KAWASUMI LABORATORIES,INC. MIE FACTORY. The authorized representative in Taiwan is Taiwan Asahi Kasei Medical Device Trading Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KAWASUMI LABORATORIES INC. MIE FACTORY, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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